NDC 85534-0004
Baclofen 20 mg tablet
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-395.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Product details
- Generic drug
- Baclofen: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA214099
- On the market since
- Jul 13, 2021
- Package NDCs
85534-0004-085534-0004-185534-0004-385534-0004-685534-0004-9- Official label
- DailyMed (National Library of Medicine), updated Jun 11, 2025
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